The Role of Electroencephalography in Caffeine Discontinuation Timing in Premature Infants
The aim of this observational study is to investigate whether functional maturation assessment by electroencephalography in preterm infants can provide reliable data for the safe discontinuation of caffeine therapy without recurrence of apnea. In preterm infants receiving caffeine therapy, an assessment of maturation w
| Condition(s) | Apnea Neonatal, Apnea of Prematurity |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | The aim of this observational study is to investigate whether functional maturation assessment by electroencephalography in preterm infants can provide reliable data for the safe discontinuation of caffeine therapy without recurrence of apnea. In preterm infants receiving caffeine therapy, an assessment of maturation will be performed by EEG at the time when discontinuation of caffeine treatment is planned. |
| Who can participate | Inclusion Criteria: 1. Infants born before 28 weeks of gestation with a birth weight of 1250 grams or less, who received prophylactic caffeine therapy. 2. Infants with a birth weight greater than 1250 grams and a gestational age below 32 weeks, who required invasive mechanical ventilation and were started on prophylactic caffeine therapy. 3. Infants born at less than 37 weeks of gestation, admitted to the neonatal intensive care unit, and treated with caffeine for apnea of prematurity. 4. Infants whose parents or legal guardians provided informed consent. Exclusion Criteria: 1. Infants who did not receive caffeine therapy, 2. Infants for whom an EEG could not be performed, 3. Infants with major congenital malformations such as neuromuscular disorders, central nervous system developmental a |
| Ages | 1 Month |
| Sex | All |
| Lead sponsor | Uludag University |
| Locations | Bursa, Turkey (Türkiye) |
| Start date | 2026-01-02 |
| NCT ID | NCT07324941 |
| Official listing | https://clinicaltrials.gov/study/NCT07324941 |